A pinch-off phenomenon is discovered in the evolution of 2D wormlike nanoclusters formed in homoepitaxial adlayers. This feature is shown to distinguish mass transport via periphery diffusion from other mechanisms. Continuum modeling of such evolution accurately describes experimental observations, particularly if one incorporates the anisotropy in step-edge line tension.
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http://dx.doi.org/10.1103/PhysRevLett.86.3088 | DOI Listing |
Carbohydr Polym
July 2024
Laboratory of Natural Materials Technology, Åbo Akademi University, Henrikinkatu 2, FI-20500 Turku, Finland. Electronic address:
As a contribution to expand accessibility in the territory of bio-based nanomaterials, we demonstrate a novel material strategy to convert amorphous xylan preserved in wood biomass to hierarchical assemblies of crystalline nanoxylan on a multi-length scale. By reducing the end group in pressurized hot water extracted (PHWE) xylan to primary alcohol as a xylitol form with borohydride reduction, the endwise-peeling depolymerization is effectively impeded in the alkali-catalyzed hydrolytic cleavage of side substitutions in xylan. Nanoprecipitation by a gradual pH decrease resulted in a stable hydrocolloid dispersion in the form of worm-like nanoclusters assembled with primary crystallites, owing to the self-assembly of debranched xylan driven by strong intra- and inter-chain H-bonds.
View Article and Find Full Text PDFEur Phys J E Soft Matter
April 2019
Department of Physics, IISER-Pune, Dr. Homi Bhabha Road, 411008, Pune, India.
Using Monte Carlo simulations, we investigate the self-assembly of model nanoparticles inside a matrix of model equilibrium polymers (or matrix of wormlike micelles) as a function of the polymeric matrix density and the excluded volume parameter between polymers and nanoparticles. In this paper, we show morphological transitions in the system architecture via synergistic self-assembly of nanoparticles and the equilibrium polymers. In a synergistic self-assembly, the resulting morphology of the system is a result of the interaction between the nanoparticles and the polymers and corresponding re-organization of both the assemblies.
View Article and Find Full Text PDFJ Phys Condens Matter
July 2010
Dipartimento di Chimica, Università di Sassari and INSTM, Unità di ricerca di Sassari, Via Vienna 2, I-07100 Sassari, Italy.
In order to study the behaviour of water adsorbed in zeolites, which are microporous crystalline aluminosilicates, whose channels and cavities of nanometric dimensions can host many different molecules, we developed a sophisticated empirical potential for water, including the full flexibility of the molecule and the correct response to the electric field generated by the cations and by the charged atoms of the aluminosilicate framework. The reproduction of experimental data by our potential model is similar or even better than that obtained from the first principles methods. The results of molecular dynamics simulations of water confined in a variety of zeolites (worm-like clusters in silicalite, spherical nanoclusters in zeolite A and ice-like nanotubes in AlPO(4)-5 and SSZ-24) at different temperatures and coverage (loading) are discussed in connection with the experimental data, whose overall good reproduction encourages the attempt of an atomic-scale description of structural and dynamical phenomena occurring in confined water, in particular in the supercooled regime.
View Article and Find Full Text PDFJ Phys Chem B
December 2005
Dipartimento di Scienze Chimiche and Unità di Ricerca INFM-CNR, Università di Padova, Via Marzolo, I-35131 Padova, Italy.
Ultrathin ordered titanium oxide films on Pt(111) surface are prepared by reactive evaporation of Ti in oxygen. By varying the Ti dose and the annealing conditions (i.e.
View Article and Find Full Text PDFLangmuir
January 2004
Chemical Engineering Department, University of Amsterdam, 1018 WV Amsterdam, The Netherlands.
Stable nanoclusters (approximately 2 nm in diameter) of copper, silver, gold, palladium, and ruthenium coated with hydrophobic coronas are easily trapped in self-assembled "soft crystal" hexagonal phase gels made of water and surfactants. The system's crystal structure and phase behavior are studied in detail. A partial phase diagram showing the hexagonal phase region for the water/SDS/toluene region is presented.
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